The Clinical Applications of D-type Parastomal Hernia Repair Surgery

NCT ID: NCT06397014

Last Updated: 2024-05-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

91 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-02-01

Study Completion Date

2023-08-01

Brief Summary

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During the period from February 2018 to February 2022, a study was conducted on patients with parastomal hernia.There were 23 patients who underwent repair surgery for D-type colostomy hernia, while 68 patients underwent traditional laparoscopic repair surgery for hernia.The inclusion criteria were: (1) preoperative diagnosis of parastomal hernia by CT scan; (2) underwent laparoscopic repair surgery or combined laparoscopic repair with abdominal wall and stoma reconstruction surgery.The exclusion criteria were: (1) occurrence of tumor recurrence and/or new tumors during the follow-up period; (2) death or loss to follow-up during the follow-up period.

Detailed Description

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Conditions

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Hernia Repair Stoma Reconstruction Function and Appearance

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

RETROSPECTIVE

Study Groups

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D-type

D-type stoma lateral hernia repair

Intervention Type PROCEDURE

underwent D-type stoma lateral hernia repair

Sugerbaker

D-type stoma lateral hernia repair

Intervention Type PROCEDURE

underwent D-type stoma lateral hernia repair

Interventions

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D-type stoma lateral hernia repair

underwent D-type stoma lateral hernia repair

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

(1) preoperative diagnosis of parastomal hernia by CT scan; (2) underwent laparoscopic repair surgery or combined laparoscopic repair with abdominal wall and stoma reconstruction surgery.

Exclusion Criteria

(1) occurrence of tumor recurrence and/or new tumors during the follow-up period; (2) death or loss to follow-up during the follow-up period.
Minimum Eligible Age

60 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Daorong Wang

OTHER

Sponsor Role lead

Responsible Party

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Daorong Wang

DR

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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Northern Jiangsu People's Hospital

Yangzhou, Jiangsu, China

Site Status

Countries

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China

Other Identifiers

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PSH001

Identifier Type: -

Identifier Source: org_study_id

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